EP2152783B1

EP2152783B1 - Medical devices comprising a co-polymer of a modified polyamide and a polycarbonate

Info

Publication number: EP2152783B1
Application number: EP08749429.0A
Authority: EP
Inventors: Günter LORENZ
Original assignee: Abbott Laboratories Vascular Enterprises Ltd
Current assignee: Abbott Laboratories Vascular Enterprises Ltd
Priority date: 2007-05-10
Filing date: 2008-05-09
Publication date: 2015-06-17
Anticipated expiration: 2028-05-09
Also published as: JP5255627B2; EP1990356A1; US8389646B2; AU2008250632B2; JP2010526894A; US20100305683A1; EP2152783A1; CN101687990A; AU2008250632A1; AU2008250632B8; WO2008138569A1; CN101687990B

Description

Field of the invention

The present invention refers to medical devices comprising a modified Co-Polymer and the modified Co-Polymer itself having high flexibility and high stress resistance, especially tensile strength or tear resistance, in addition to the good physical characteristics of a Block-Co-Polymers of a polyamide and a polycarbonate, either polycarbonate diol or polycarbonate diamine.

Background of the invention

Block-Co-Polymers of a polyamide and a polyether have been used in the polymer industry for a long time and - due to their enormous range of possible applications - are found in many branches of industrial products. Recently in the area of medicinal devices good use has been made of these materials especially in implants. The most popular Block-Co-Polymer of a polyamide and a polyether used in this field is PEBAX^™, besides the polyamides, which include different sorts of Nylons. Even though these materials have certainly been used successfully, due to the strains put on the materials and the necessity to improve their characteristics in the light of growing experience coming from increasing numbers of treated patients, there clearly is a need for improved materials/elastomers allowing for an effective treatment of the patient preferably with an economical production process.

Summary of the invention

It is an object of the current invention to provide medical devices comprising modified elastomers or the modified elastomers themselves, preferably Co-Polymers having high flexibility and high stress resistance, especially tensile strength or tear resistance in addition to the good physical characteristics of the Co-Polymers.
The invention thus refers to the use of a Co-Polymer producible by polymerizing a modified polyamide with a polycarbonate diol or a polycarbonate diamine, characterized in that the modified polyamide is producible by contacting/mixing one or more pre-polyamides with an at least mono-substituted α,ω-di-carboxylic acid or its alkyl ester or its acyl halides and raising the temperature to above 150° C in the production of implants or medical devices.
The invention further resides in the use of a Co-Polymer according to general formula X, Xa, Xb, Xc or XI, XIa, XIb, XIc
or
or
or

or
or
or
in the production of implants or medical devices.
The invention furthermore resides in the use according to the invention in the production of medical devices, balloon material, stents, stent grafts, and catheters.

Detailed Description of the invention

The use of stents, balloons, catheters and other medical devices etc. in minimal invasive surgery, especially in the cardiovascular field, has in the last years shown a high growth. As a consequence the need for useful materials fulfilling highly specialized needs in the field of different medicinal devices has clearly risen in a technical area, which traditionally is more governed by bulk products. Especially in the field of balloons used cardiovascular surgery there was a clear desire for an elastomer, which is on one hand flexible enough to be introduced into a vascular environment without causing damage, while on the other hand being stable and rigid enough, especially in the moment of actual surgery, and inflation in the vessel, to not be extended too much inside the vessel. Besides that, the material should also have a low water absorption, because its physicochemical properties, while used or while on the shelf could be severely hampered by accepting too much water, as it could also be hampered by changes during storage due to thermo-oxidation.
WO02/074194A2 discloses stents having medicated multilayer hybrid polymer coatings mentioning polyamide copolymers.
The invention thus refers to the use of a Co-Polymer producible by polymerizing a modified polyamide with a polycarbonate diol or a polycarbonate diamine, characterized in that the modified polyamide is producible by contacting/mixing one or more pre-polyamides with an at least mono-substituted α,ω-di-carboxylic acid or its alkyl ester or its acyl halides and raising the temperature to above 150° C in the production of an implant or medical device.
Preferably the implant or medical device according to the invention is selected from implanted or implantable medical devices, from balloon/balloon material, stents, stent grafts, grafts graft connectors or catheters.
Also the implant or medical device according to the invention may be selected from implanted or implantable medical devices or minimal invasive medical devices, from stents, stent grafts, grafts, graft connectors, closure devices, filters, or catheters, delivery catheters, stent delivery catheters, balloon dilatation catheters or medical balloons/balloon material.
In an additional embodiment the implant or medical device according to the invention is an implanted, implantable or minimal invasive medical device, preferably is a balloon, or stent, stent graft, graft, graft connector or catheter; more preferably is a balloon catheter or a medical balloon for a medical device, most preferably is a medical balloon for a balloon catheter.
Also in one embodiment the implant or medical device according to the invention is an implanted, implantable or minimal invasive medical device, preferably is a balloon, more preferably is a balloon catheter or a medical balloon for a medical device, most preferably is a medical balloon for a balloon catheter.
"Balloon or balloon material" in the context of this invention especially means a balloon used in coronary balloon angioplasty and the material used for these balloons, especially balloon catheters. In this, e.g. a balloon catheter is inserted into an artery and advanced to e.g. a narrowing in a coronary artery. The balloon is then inflated to enlarge the lumen. Especially it means balloon of a balloon catheter used in minimally invasive interventions, preferably in vascular interventions, more preferably used in coronary or endovascular balloon angioplasty and the material used for these balloons. Non-invasive procedures such as percutaneous transluminal angioplasty (PTA), percutaneous transluminal coronary angioplasty (PTCA), stent delivery and deployment, radiation treatment, delivery of a drug at a lesion site and other procedures are used in the treatment of intravascular disease. These therapies are well known in the art and usually utilize a balloon catheter pulled over a guide wire. After a guiding catheter is placed into the patient's main vessel, a guide wire is advanced in the guide catheter and beyond the distal end of the guide catheter. The balloon catheter is then advanced over the guidewire until it reaches the treatment site at the lesion or stenosis. The balloon is inflated to compress the lesion site and dilate the previous narrowed lesion or stenosis site. If the balloon carried a stent and/or drug, the stent and/or drug is delivered at the site when the balloon is inflated. Likewise, further therapies may also use a balloon catheter for the treatment of the lesion site.
"Stent" means an elongate implant with a hollow interior and at least two orifices and usually a circular or elliptical, but also any other, cross section, preferably with a perforated, lattice-like structure that is implanted into vessels, in particular blood vessels, to restore and maintain the vessels patent and functional.
"Graft" means an elongate implant with a hollow interior and with at least two orifices and usually circular or elliptical, but also any other, a cross section and with at least one closed polymer surface which is homogeneous or, optionally, woven, braided, knitted or spun from various strands. The surface preferably is impermeable to corpuscular constituents of blood and/or for water, so that the implant serves as a vascular prosthesis and is usually employed for damaged vessels or in place of vessels.
"Stent graft" means a connection between a stent and a graft. A stent graft preferably comprises a vascular prosthesis reinforced with a stent (both as defined above), wherein a polymer layer is homogeneous or, optionally, woven from various strands and is impermeable for corpuscular constituents of blood and/or for water. Especially the stent graft may be woven, braided, knitted or spun from various strands and may be impermeable for corpuscular constituents of blood and/or for water or may be porous to allow endothelial ingrowth but impermeable to release of emboli or may function as a mere filter for emboli. More preferably, the stent has on at least 20% of its surface a perforated (lattice-like), preferably metallic, outer layer and at least one closed polymer layer that is located inside and/or outside the stent outer layer, or, optionally, is woven, braided, knitted or spun from various strands and may be impermeable for corpuscular constituents of blood and/or for water or may be porous to allow endothelial ingrowth but impermeable to release of emboli or may function as a mere filter for emboli.. Optionally, where the closed polymer layer is disposed inside the metallic outer layer, a further perforated (lattice-like), preferably metallic, inner layer may be located inside the polymer layer.
"Graft connector" means an implant that connects at least two hollow organs, vessels or grafts, consists of the materials defined for grafts or stent grafts and/or has the structure defined for the latter. Preferably, a graft connector has at least two, three or four, orifices, arranged, for example, as an asymmetric "T" shape.
"Catheter" means a tubular instrument intended for introduction into hollow organs. More preferably, a catheter may be designed for use in guiding other catheters, or for angiography, ultrasound imaging, or - especially - balloon catheters for dilatation or stent delivery. This includes also a "Catheter pump" meaning a catheter provided on its tip with a propeller able to assist the pumping of the myocardium.
Most preferably the Co-Polymer used according to the invention being comprised within the implant or medical device according to the invention is used to form a medical balloon for a medical device, especially situated on or in the medical device, especially a medical balloon situated on or in a balloon catheter, which is either a balloon catheter for stent delivery or a balloon catheter for dilation, thus carrying no stent.
Accordingly, the invention also refers to a balloon for a medical device formed from a Co-Polymer according to the invention. Preferably the balloon for a medical device is formed from a length of polymer tubing by radial expansion of the tubing under pressure, the polymer being a Co-Polymer according to the invention. Even more preferably this balloon for a medical device is formed from a length of polymer tubing by radial expansion of the tubing under pressure, the polymer being a Co-Polymer producible by polymerizing a modified polyamide with a polycarbonate diol or a polycarbonate diamine, characterized in that the modified polyamide is producible by contacting/mixing one or more pre-polyamides with an at least mono-substituted α,ω-di-carboxylic acid or its alkyl ester or its acyl halides and raising the temperature to above 150° C.
Especially for these embodiments it is preferable if the Co-Polymer from which the medical balloon is formed is showing certain attributes. Accordingly, for these embodiments it is preferred if the Co-Polymer according to the invention is showing one or both of the attributes listed below:

the Co-Polymer has a flexural modulus of less than about 150,000 psi; and/or
the Co-Polymer has a hardness, Shore D scale, of greater than 60.

In addition it is also preferable for these specific embodiments if the medical balloon according to the invention is showing one or both of the attributes listed below:

a wall strength of at least 18,000 psi, and/or
a distension over the range of 88-235 psi of at least 12%

Also it is preferable for these specific embodiments if the medical balloon according to the invention is formed by any of the following methods with the medical balloon having proximal and distal waist portions and a central body portion:

1) radially expanding a length of polymer tubing (of the Co-Polymer according to the invention) under pressure, with said length of tubing having a proximal and distal portions which are stretched to a reduced diameter and an unstretched central portion, and said radially expanding step is accomplished by expanding said tubing in a mold such that the balloon body is formed from the unstretched central portion of the tubing and the proximal and distal waist portions of the balloon are formed from the stretched proximal and distal portions of the tubing; and/or
2) extruding a tubular segment of thermoplastic material (of the Co-Polymer according to the invention) having a predetermined wall thickness and length, the segment having a proximal end, a distal end and a center portion;
drawing the segment to a predetermined length while maintaining the temperature of the segment below the highest glass transition temperature of the Co-Polymer, wherein the proximal end forms a first waist; and
expanding the segment having a first waist in a mold to produce the balloon, the balloon having a body portion, wherein the center portion of said segment becomes the balloon body portion.

The Co-Polymer producible by polymerizing a modified polyamide with a polycarbonate diol or a polycarbonate diamine, is characterized in that the modified polyamide is producible by contacting/mixing one or more pre-polyamides with an at least mono-substituted α,ω-di-carboxylic acid or its alkyl ester or its acyl halides and raising the temperature to above 150° C.
In a preferred embodiment the polymerization resulting in the Co-Polymer used according to the invention also being comprised in the implants or medical devices according to the invention is done by contacting/mixing the modified polyamide with the polycarbonate diol or polycarbonate diamine, preferably in the presence of a catalyst, preferably a Lewis base or a Lewis acid and raising the temperature to

either above 150°C in case of a melt polymerization or
above 50°C in case of a polymerization in solution.

In a preferred embodiment - preferably drawn to the case of polymerization in solution - the raising of the temperature in the polymerization resulting in the Co-Polymer used according to the invention also being comprised in the implants or medical devices according to the invention is done

a) already during the mixing/contacting and/or
b) under protective gas atmosphere, preferably under argon and/or
c) to a temperature above 200° C, preferably above 220°C and/or
d) in 2 steps with different temperatures preferably divided by an intermediate step in which the second temperature is reached within a certain time limit and/or
e) over a time period of more than 3 h, preferably of more than 4h.

In a preferred embodiment - preferably drawn to the case of melt polymerization - the raising of the temperature in the polymerisation resulting in the Co-Polymer used according to the invention also being comprised in the implants or medical devices according to the invention is done

a) under protective gas atmosphere, preferably under argon.

In a preferable embodiment of the Co-polymer used according to the invention or of the implant or medical device comprising this Co-Polymer the modified polyamide is polymerized with the polycarbonate diol or polycarbonate diamine in a molar ratio of 0.9 to 1.1, preferably in equimolar amounts.
The modified polyamide forming a part of the Co-Polmers used according to the invention also being comprised in the implants or medical devices according to the invention is producible by contacting/mixing one or more pre-polyamides, with an at least mono-substituted α,ω-di-carboxylic acid or its alkyl ester and heating to a temperature above 150° C
In a preferred embodiment the heating for the production of the modified polyamide is done

Most preferably the mixing is done under protective gas atmosphere - preferably under argon - in a first heating step at more than 200° C - preferably 220°C - for more than 1h - preferably 2h. The temperature was consequently raised within 10 to 30 min - preferably within 20 min - to more than 220°C -preferably to 250 ° C - and the mixture was stirred for another 2h.
There are 3 kinds of material used nowadays for medical devices, especially balloons, over which the material of the current invention - if compared case by case - shows advantages.

a) Nylon: Over Nylon, coming in different sorts, especially Nylon-12, the Co-Polymers of the invention show the advantage, that they are more flexible and/or have a lower water absorption. Especially the lack of flexibility is often considered as a drawback in medical devices using Nylon.
b) PEBA: Over PEBA (e.g. PEBAX^®) the Co-Polymers of the invention show the advantage, that they are slightly more rigid and/or have a lower water absorption, again making them superior for the intended special use and allowing a much needed compromise balancing flexibility and rigidity. In addition the material of the invention seems to show higher stability, especially if compared to the effects of thermo-oxidation shown by PEBA and/or also an improved dimensional stability.
c) Blend of a) and b): The need for a compromise between the higher rigidity of Nylon and higher flexibility of PEBA has already resulted in blends being used. Still, these have no defined structures or phases, giving the material of the inventions which seems to have a lower water absorption also already an inherent advantage.

In the context of this invention "contacting/mixing" is understood as placing the at least 2 substances (e.g. pre-polyamide and acid or modified polyamide and polycarbonate) in physical contact, e.g. in a common container, optionally mixing them to increase the amount of areas in contact between the substances.
In the context of this invention "polymerizing" is understood as a process of reacting monomers or building blocks together to form a network of polymer chains under suitable reaction conditions.
In the context of this invention "alkyl ester" of the at least mono-substituted α,ω-dicarboxylic acid is understood as an ester between the acid function on one end of the acid and a C_1-6-alkyl group.
In the context of this invention "acyl halide" of the at least mono-substituted α,ω-dicarboxylic acid is understood as the replacement of a hydroxyl group in the acid function by a halogen atom (-C(O)-X) - preferably a chlorine atom.
Generally "at least monsubstituted" means either "monosubstituted" or "polysubstituted".
An "aryl", "aryl radical" or group is understood as meaning ring systems with at least one aromatic ring but without heteroatoms even in only one of the rings. Examples are phenyl, naphthyl, fluoranthenyl, fluorenyl, tetralinyl or indanyl, in particular 9H-fluorenyl or anthracenyl radicals, which can be unsubstituted or monosubstituted or polysubstituted.
In the context of this invention "cycloalkyl radical" or group is understood as meaning saturated and unsaturated (but not aromatic) cyclic hydrocarbons (without a heteroatom in the ring), which can be unsubstituted or mono- or polysubstituted. Furthermore, C_3-4-cycloalkyl represents C₃- or C₄-cycloalkyl, C_3-5-cycloalkyl represents C₃-, C₄- or C₅-cycloalkyl, C_3-6-cycloalkyl represents C₃-, C₄-, C₅- or C₆-cycloalkyl, C_3-7-cycloalkyl represents C₃-, C₄-, C₅-, C₆- or C₇-cycloalkyl, C_3-8-cycloalkyl represents C₃-, C₄-, C₅-, C₆-, C₇- or C₈-cycloalkyl, C_4-5-cycloalkyl represents C₄- or C₅-cycloalkyl, C_4-6-cycloalkyl represents C₄-, C₅- or C₆-cycloalkyl, C_4-7-cycloalkyl represents C₄-, C₅-, C₆- or C₇-cycloalkyl, C_4-8-cycloalkyl represents C₄-, C₅-, C₆- C₇- or C₈-cycloalkyl C_5-6-cycloalkyl represents C₅- or C₆-cycloalkyl and C_5-7-cycloalkyl represents C₅-, C₆- or C₇-cycloalkyl. However, mono- or polyunsaturated, preferably monounsaturated, cycloalkyls also in particular fall under the term cycloalkyl as long as the cycloalkyl is not an aromatic system. The cycloalkyl radicals are preferably cyclopropyl, 2-methylcyclopropyl, cyclopropylmethyl, cyclobutyl, cyclopentyl, cyclopentylmethyl, cyclohexyl, cycloheptyl, cyclooctyl, and also adamantly.
A "heterocyclyl", a "heterocyclyl radical" or group or "heterocyclic ring system" is understood as meaning heterocyclic ring systems which contain one or more heteroatoms from the group consisting of nitrogen, oxygen and/or sulfur in the ring or ringsystem, and can also be mono- or polysubstituted. The ringsystem may consist either of only one saturated or unsaturated or even aromatic ring or may consist of 2, 3 or 4 saturated or unsaturated or even aromatic rings, which are condensed in that between two or more of the rings ring members are shared. Examples which may be mentioned from the group of heterocyclyls are furan, benzofuran, thiophene, benzothiophene, pyrrole, pyridine, pyrimidine, pyrazine, quinoline, isoquinoline, phthalazine, benzo-1,2,5-thiadiazole, imidazo-thiazole, benzothiazole, indole, benzotriazole, benzodioxolane, benzodioxane, carbazole and quinazoline.
In connection with aryl radical, cycloalkyl radical, or heterocyclyl radical, "substituted" is understood - unless defined otherwise - as meaning replacement of at least one hydrogen radical on the ring-system of the aryl radical, the cycloalkyl radical, or the heterocyclyl radical by OH, SH, =O, halogen (F, Cl, Br, I), CN, NO₂, COOH; NR_xR_y, with R_x and R_y independently being either H or a saturated or unsaturated, linear or branched, substituted or unsubstituted C_1-6-alkyl; by a saturated or unsaturated, linear or branched, substituted or unsubstituted C_1-6-alkyl; a saturated or unsaturated, linear or branched, substituted or unsubstituted -O-C_1-6-alkyl (alkoxy); a saturated or unsaturated, linear or branched, substituted or unsubstituted -S-C_1-6-alkyl; a saturated or unsaturated, linear or branched, substituted or unsubstituted -C(O)-C_1-6-alkyl; a saturated or unsaturated, linear or branched, substituted or unsubstituted -C(O)-O-C_1-6-alkyl; a substituted or unsubstituted phenyl. "Optionally at least monsubstituted" means either "not substituted" if the option is not fulfilled, "monosubstituted" or "polysubstituted", and "at least monsubstituted" means either "monosubstituted" or "polysubstituted".
Aliphatic radicals/groups, as referred to in the present invention, are optionally mono- or polysubstituted and may be branched or unbranched, saturated or unsaturated. Aliphatic radicals, as defined in the present invention, include alkyl, alkenyl and alkinyl radicals. Unsaturated aliphatic radicals, as defined in the present invention, include alkenyl and alkinyl radicals. Preferred aliphatic radicals according to the present invention include but are not restricted to methyl, ethyl, vinyl (ethenyl), ethinyl, propyl, n-propyl, isopropyl, allyl (2-propenyl), 1-propinyl, methylethyl, butyl, n-butyl, iso-butyl, sec-butyl, tert-butyl butenyl, butinyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, n-pentyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, hexyl, 1-methylpentyl, n-heptyl, n-octyl, n-nonyl and n-decyl.
In the context of this invention, alkyl radical or group is understood as meaning saturated and unsaturated, linear or branched hydrocarbons, which can be unsubstituted or mono- or polysubstituted. Thus unsaturated alkyl is understood to encompass alkenyl and alkinyl groups, like e.g. -CH=CH-CH₃ or -CΞC-CH₃, while saturated alkyl encompasses e.g. -CH₃ and -CH₂-CH₃. In these radicals, C_1-2-alkyl represents C₁- or C₂-alkyl, C_1-3-alkyl represents C₁-, C₂- or C₃-alkyl, C_1-4-alkyl represents C₁-, C₂-, C₃- or C₄-alkyl, C_1-5-alkyl represents C₁-, C₂-, C₃-, C₄-, or C₅-alkyl, C_1-6-alkyl represents C₁-, C₂-, C₃-, C₄-, C₅- or C₆-alkyl, C_1-7-alkyl represents C₁-, C₂-, C₃-, C₄-, C₅-, C₆- or C₇-alkyl, C_1-8-alkyl represents C₁-, C₂-, C₃-, C₄-, C₅-, C₆-, C₇- or C₈-alkyl, C_1-10-alkyl represents C₁-, C₂-, C₃-, C₄-, C₅-, C₆-, C₇-, C₈-, C₉- or C₁₀-alkyl and C_1-18-alkyl represents C₁-, C₂-, C₃-, C₄-, C₅-, C₆-, C₇-, C₈-, C₉-, C₁₀-, C₁₁-, C₁₂-, C₁₃-, C₁₄-, C₁₅-, C₁₆-, C₁₇- or C₁₈-alkyl. The alkyl radicals are preferably methyl, ethyl, vinyl (ethenyl), propyl, allyl (2-propenyl), 1-propinyl, methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, hexyl, 1-methylpentyl, if substituted also CHF₂, CF₃ or CH₂OH etc.
In connection with alkylene, alkyl or aliphatic radical or group - unless defined otherwise - the term "substituted" in the context of this invention is understood as meaning replacement of at least one hydrogen radical by F, Cl, Br, I, NH₂, SH or OH; within that "monosubstituted" means the substitution of exactly one hydrogen radical, whereas "polysubstituted" means the substitution of more than one hydrogen radical with "polysubstituted" radicals being understood as meaning that the replacement takes effect both on different and on the same atoms several times with the same or different substituents, for example three times on the same C atom, as in the case of CF₃, or at different places, as in the case of e.g. -CH(OH)-CH=CH-CHCl₂. Therefore, "optionally at least monsubstituted" means either "not substituted" if the option is not fulfilled, "monosubstituted" or "polysubstituted", and "at least monsubstituted" means either "monosubstituted" or "polysubstituted". This definition of "substituted" or the selected substituents generally also applies to the "at least mono-substituted α,ω-di-carboxylic acid or its alkyl ester or its acyl halides" or an acid of formula I.
The term "alkylene" is understood as meaning a divalent alkyl group like -CH₂- or-CH₂-CH₂- with (CH₂)_3-6 being understood as meaning -CH₂-CH₂-CH₂-, -CH₂-CH₂-CH₂-CH₂-, -CH₂-CH₂-CH₂-CH₂-CH₂- and -CH₂-CH₂-CH₂-CH₂-CH₂-CH₂-, (CH₂)_1-4 is to be understood as meaning -CH₂-, -CH₂-CH₂-, -CH₂-CH₂-CH₂- and -CH₂-CH₂-CH₂-CH₂-, (CH₂)_4-5 is to be understood as meaning -CH₂-CH₂-CH₂-CH₂- and -CH₂-CH₂-CH₂-CH₂-CH₂-, etc.
In a preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the at least mono-substituted α,ω-di-carboxylic acid is selected from at least mono-substituted oxalic acid, malonic acid, succinic acid, fumaric acid, glutaric acid, adipic acid, 1,7-heptane-dicarboxylic acid, 1,8-octane-di-carboxylic acid, 1,9-nonane-di-carboxylic acid, 1,10-decane-di-carboxylic acid, 1,11-undecane-di-carboxylic acid, 1,12-dodecane-di-carboxylic acid; preferably from at least mono-substituted adipic acid or 1,10-decane-di-carboxylic acid.
In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the at least mono-substituted α,ω-di-carboxylic acid is selected from at least mono-substituted malonic acid, succinic acid, fumaric acid, glutaric acid, adipic acid, 1,7-heptane-dicarboxylic acid, 1,8-octane-di-carboxylic acid, 1,9-nonane-di-carboxylic acid, 1,10-decane-dicarboxylic acid, 1,11-undecane-di-carboxylic acid, 1,12-dodecane-di-carboxylic acid; preferably from at least mono-substituted adipic acid or 1,10-decane-di-carboxylic acid.
In the context of this invention "forming a part of the Co-Polymer used according to the invention" is defined as the compound "forming a part" being the source of a building block or building blocks derived from this compound during the production of the Co-Polymer according to the invention. Thus, these building blocks are being part of the used Co-polymer after the final production step (e.g. the polymerisation).
In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the at least mono-substituted α,ω-di-carboxylic acid is a compound of general formula I

HOOC-(CH₂)_m-CHR¹-(CH₂)_n-COR² (I)

wherein

m and n are independently from each other selected from a natural number and 0 and n + m is between 1 and 9, preferably between 3 and 7;
R² is selected from OH, halogen or OC_1-4-alkyl;
R¹ is any radical except hydrogen, preferably is a sterically voluminous group.

In the context of this invention a "sterically voluminous group" is understood as a radical that due to its steric effect, derived from the amount of space occupied by atoms of the molecule, does give a relatively high effect of steric hindrance. Steric effects arise from the fact that each atom within a molecule occupies a certain amount of space. If atoms are brought too close together, there is an associated cost in energy, and this may affect the molecule's preferred shape and chemical reaction. Steric hindrance occurs when the size of groups within a molecule prevents chemical reactions that are observed in related smaller molecules or may also restrict molecular geometry between adjacent groups.
In another preferred embodiment of the modified polyamide according to formula I forming a part of the Co-Polymer used according to the invention
either
m and n are independently from each other selected from 0, 1, 2 or 3 and n + m is 3;
or
m and n are independently from each other selected from 0, 1, 2, 3, 4, 5, 6 or 7 and n + m is 7;
preferably wherein
m and n are independently from each other selected from 0, 1, 2 or 3 and n + m is 3.
In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the at least mono-substituted α,ω-di-carboxylic acid is a compound of general formula II
wherein

one of R^3' and R³ is selected from hydrogen, while the other may be either hydrogen or C_1-4-alkyl;
0, 1 or 2 of the bonds marked by a dotted line ---------- may be a double bond, with the proviso, that if there are 2 double bonds they may not touch the same C-atom;
R¹ is any radical except hydrogen, preferably is a sterically voluminous group.

In another preferred embodiment of the modified polyamide used according to either formula I or II forming a part of the Co-Polymer according to the invention
R¹ is selected from halogen; a branched or linear, saturated or non-saturated, optionally substituted C_1-6 aliphatic radical; an optionally substituted aryl; a saturated or non-saturated, optionally substituted C_3-10-cycloalkyl; an optionally substituted heterocyclyl.
In the preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the at least mono-substituted α,ω-di-carboxylic acid is 3-tert. butyl adipic acid.
In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the pre-polyamide is a structure of general formula III or IIIa
or

, preferably a structure of general formula III
, wherein

A is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally at least one carbon atom being replaced by NH, O or S; preferably is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;
A' is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally at least one carbon atom being replaced by NH, O or S; preferably is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;
B and B' independently from one another are selected from H or C_1-4-Alkyl;
v is a natural number between 1 and 24;
v' is a natural number between 1 and 24;
y is a natural number ≥1.

In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention in the pre-polyamide according to general formula III or IIIa

A is a branched or linear, saturated or non-saturated, optionally substituted divalent aliphatic group; preferably is optionally substituted alkylene; more preferably is - CH₂ -;
A' is a branched or linear, saturated or non-saturated, optionally substituted divalent aliphatic group; preferably is optionally substituted alkylene; more preferably is - CH₂ -;
and/or
v is a natural number between 3 and 13, preferably is a natural number between 5 and 11; more preferably is 5, 10 or 11, most preferably is 11 or 5;
v' is a natural number between 3 and 13, preferably is a natural number between 5 and 11; more preferably is 5, 10 or 11, most preferably is 11 or 5;
preferably,

A is a branched or linear, saturated or non-saturated, optionally substituted divalent aliphatic group; preferably is optionally substituted alkylene; more preferably is - CH₂ -;
and/or
v is a natural number between 3 and 13, preferably is a natural number between 5 and 11; more preferably is 5, 10 or 11, most preferably is 11.

In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the pre-polyamide is selected from Nylon 6; Nylon 6,6; Nylon 11; or Nylon 12; preferably is Nylon 12.
In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the pre-polyamide is selected from Nylon 6; Nylon 6,6; Nylon 11; or Nylon 12; preferably is Nylon 12
and
the at least mono-substituted α,ω-di-carboxylic acid is 3-tert. butyl adipic acid.
In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the at least mono-substituted α,ω-di-carboxylic acid is added - when producing the modified polyamide - in an amount resulting in a molar ratio between the acid and the pre-polyamide (wherein the molarity of the pre-polyamide is calculated relatively based on the equivalent number of theoretical lactam units in the pre-polyamide) of

between 0.05 and 0.0005, preferably between 0.025 and 0.001; or
between 1.0 and 0.0005, preferably between 0.75 and 0.00075, and more preferably between 0.5 and 0.001, or between 0.05 and 0.004, or between 0.1 and 0.001.

In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the at least mono-substituted α,ω-di-carboxylic acid is added - when producing the modified polyamide - in an amount resulting in a molar ratio between the acid and the pre-polyamide calculated (wherein the molarity of the pre-polyamide is calculated relatively based on the number and molecular weight of polymerized amide building blocks (VIII))
and the molar ratio results in

Thus, e.g. if mixing Y grams of di-carboxylic acid and X grams of pre-polyamide, the amount of acid is divided by its molecular weight to give the molarity, while the amount of pre-polyamide is divided by the molecular weight of the building block/the theoretical basic lactam unit to give its relative molarity. Then the relative molecular ratio of acid : pre-polyamide is calculated.
In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the reaction leading to the modified polyamide is executed using reactive extrusion as described in DD 276 290 A1 and Eichhorn et al. (Journal of Applied Polymer Science, Vol. 62, 2053-2060 (1996).
In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the modified polyamide is of general formula IV or IVa
or
, preferably IV,
wherein

A is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally at least one carbon atom being replaced by NH, O or S; preferably is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;
A' is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally at least one carbon atom being replaced by NH, O or S; preferably is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;
B and B' independently from one another are selected from H or C_1-4-Alkyl;
v is a natural number between 1 and 24;
v' is a natural number between 1 and 24;
y is a natural number ≥1;
y' is a natural number ≥1 or 0;
m and n are independently from each other selected from 0 and a natural number between 1 and 9 and n + m is a natural number between 1 and 9; and
R¹ is any radical except hydrogen, preferably is a sterically voluminous group.

In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the modified polyamide is of general formula V
, wherein

B and B' independently from one another are selected from H or C_1-4-Alkyl;
v is a natural number between 1 and 24;
y is a natural number ≥1.
y' is a natural number ≥1 or 0;
R¹ is selected from halogen; a branched or linear, saturated or non-saturated, optionally substituted C_1-6 aliphatic radical; an optionally substituted aryl; a saturated or non-saturated, optionally substituted C_3-10-cycloalkyl; an optionally substituted heterocyclyl.

In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the modified polyamide is of general formula IV or V, wherein

B and B' are hydrogen;
and/or
v is a natural number between 3 and 13, preferably is a natural number between 5 and 11; preferably is 5, 10 or 11, more preferably is 5 or 11, most preferably is 11;
and/or
y' is 0;
and/or
y + y' is between 20 and 2000, preferably 40 and 1000;
and/or
R¹ is selected from halogen; a branched or linear, saturated or non-saturated, optionally substituted C_1-4 alkyl-radical, preferably is iso-propyl or tert. butyl, more preferably is tert. butyl.

In another preferred embodiment of the modified polyamide forming a part of the Co-Polymer used according to the invention the modified polyamide is of general formula V, wherein

v is 11;
and
R¹ is tert. butyl.

In another preferred embodiment of the polycarbonate forming a part of the Co-Polymer used according to the invention the polycarbonate is a polycarbonate diol of general formula VI or VIa

or the polycarbonate is a polycarbonate diamine of general formula VII or VIIa

wherein

E is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain;
B and B' independently from one another are selected from H or C_1-4-Alkyl;
w is a natural number between 1 and 24;
z is a natural number ≥1.

In another preferred embodiment of the polycarbonate forming a part of the Co-Polymer used according to the invention the polycarbonate is a polycarbonate diol of general formula VIa or a polycarbonate diamine of general formula VIIa
, wherein

B and B' are hydrogen;
w is a natural number between 1 and 10; preferably if z =1, w is a natural number between 1 and 10 and if z ≠ 1, w is a natural number between 2 and 10;
and/or
z is a natural number between 1 and 2000, preferably between 2 and 2000, more preferably between 1 and 1000.

In another preferred embodiment of the Co-polymer used according to the invention

either the reaction leading to the modified polyamide; or
the polymerization reaction; or
both reactions

DD 276 290 A1

Eichhorn et al. (Journal of Applied Polymer Science, Vol. 62, 2053-2060 (1996

Another aspect the invention relates to the use of a Co-Polymer (B) according to general formula X, Xa, Xb, Xc or XI, XIa, XIb, XIc
or

or
, wherein

A is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally at least one carbon atom being replaced by NH, O or S; preferably is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;
A' is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally at least one carbon atom being replaced by NH, O or S; preferably is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;
E is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain;
B and B' independently from one another are selected from H or C_1-4-Alkyl;
v is a natural number between 1 and 24;
v' is a natural number between 1 and 24;
w is a natural number between 1 and 24;
x is a natural number ≥1;
y and y' are independently of one another a natural number ≥1;
z is a natural number ≥1;
m and n are independently from each other selected from 0 and a natural number between 1 and 9 and n + m is a natural number between 1 and 9; and
R¹ is any radical except hydrogen, preferably is a sterically voluminous group in the production of the implants or medical devices according to the invention.

In another preferred embodiment of the Co-Polymer (B) used for the production of the implants or medical devices according to the invention the Co-Polymer is of general formula XII, Xlla or XIII, Xllla
or
, wherein

B and B' independently from one another are selected from H or C_1-4-Alkyl;
v is a natural number between 1 and 24;
w is a natural number between 1 and 24;
x is a natural number ≥1;
y and y' are independently from one another a natural number ≥1;
z is a natural number ≥1;
R¹ is selected from halogen; a branched or linear, saturated or non-saturated, optionally substituted C_1-6 aliphatic radical; an optionally substituted aryl; a saturated or non-saturated, optionally substituted C_3-10-cycloalkyl; an optionally substituted heterocyclyl.

In another preferred embodiment of the Co-Polymer (B) used according to the invention according to general formula X, Xa, Xb, Xc, or XI, XIa, XIb, XIc or XII, Xlla or XIII, XIIIa in the Co-Polymer

B and B' are hydrogen;
and/or
v is a natural number between 3 and 13, preferably is a natural number between 5 and 11; preferably is 5, 10 or 11, more preferably is 5 or 11, most preferably is 11;
and/or
w is a natural number between 1 and 10; preferably if z =1, w is a natural number between 1 and 10 and if z ≠ 1, w is a natural number between 2 and 10;
and/or
z is a natural number between 1 and 2000, preferably between 2 and 2000, more preferably between 1 and 1000;
and/or
y is a natural number between 1 and 2000, preferably 2 and 1000, more preferably between 2 and 200, even more preferably between 2 and 150, most preferably between 2 and 100;
and
y' is a natural number between 1 and 2000, preferably 2 and 1000, more preferably between 2 and 200, even more preferably between 2 and 150, most preferably between 2 and 100;
and
the sum of y + y' is a natural number between 1 and 2000, preferably between 2 and 1000, more preferably between 2 and 200, even more preferably between 2 and 150, most preferably between 2 and 100;
and/or
x is a natural number between 1 and 100;
and/or
R¹ is selected from halogen; a branched or linear, saturated or non-saturated, optionally substituted C_1-4 alkyl-radical, preferably is iso-propyl or tert. butyl, more preferably is tert. butyl.

In another preferred embodiment of the Co-Polymer (B) used according to the invention according to general formula XII or XIII in the Co-Polymer (B)

v is 11;
and
R¹ is tert. butyl.

In another preferred embodiment of the Co-Polymer used according to the invention the Co-Polymer is modified in at least one of the end groups with liquid crystalline oligomers (LCOs/LC-oligomers).
Another aspect of the invention provides the use of a Co-Polymer (C) in the production of implants or medical devices according to the invention comprising units derived from polyamide-forming monomers, units derived from polycarbonate diols or polycarbonate diamines and units derived from at least mono-substituted α,ω-di-carboxylic acids,
wherein the polyamide-forming monomers are represented by the following formulas (IX) or (IXa), the polycarbonate diols are represented by the following formulas (VI) or (VIa), polycarbonate diamines are represented by the following formula (VII) or (VIIa) and the at least mono-substituted α-ω-di-carboxylic acids are represented by the following formula (I):
, wherein

A is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S; preferably is methylene,
and
v is a natural number between 1 and 24; preferably is a natural number between 3 and 13, more preferably is a natural number between 5 and 11; more preferably is 5, 10 or 11, even more preferably is 5 or 11, most preferably is 11;
with

or

, wherein
E is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain; preferably is methylene;
B and B' independently from one another are selected from H or C_1-4-Alkyl; preferably are H
w is a natural number between 1 and 24;
z is a natural number ≥1;
with

HOOC-(CH₂)_m-CHR¹-(CH₂)_n-COR² (I)

wherein
m and n are independently from each other selected from a natural number and 0 and n + m is between 1 and 9, preferably between 3 and 7; more preferably n + m is 3;
R² is selected from OH, halogen or OC_1-4-alkyl; preferably is OH;
R¹ is any radical except hydrogen, preferably is a sterically voluminous group, more preferably is selected from halogen; a branched or linear, saturated or non-saturated, optionally substituted C_1-4 alkyl-radical, even more preferably is iso-propyl or tert. butyl, most preferably is tert. butyl.

In a preferred embodiment of the Co-polymer (C) used according to the invention outlined above.

A is CH₂;
and/or
E is CH₂;
and/or
B and B' are hydrogen;
and/or
v is a natural number between 3 and 13, preferably is a natural number between 5 and 11; preferably is 5, 10 or 11, more preferably is 5 or 11, most preferably is 11;
and/or
w is a natural number between 1 and 10; preferably if z =1, w is a natural number between 1 and 10 and if z ≠ 1, w is a natural number between 2 and 10;
and/or
z is a natural number between 1 and 2000, preferably between 2 and 2000, more preferably between 1 and 1000;
and/or
R¹ is selected from halogen; a branched or linear, saturated or non-saturated, optionally substituted C_1-4 alkyl-radical, preferably is iso-propyl or tert. butyl, more preferably is tert. Butyl;
and/or
m and n are independently from each other selected from a natural number and 0 and n + m is between 1 and 9, preferably between 3 and 7;
and/or
R² is selected from OH, halogen or OC_1-4-alkyl.

In a preferred embodiment of the Co-Polymer (C) used according to the invention outlined above the Co-Polymer contains the units derived from polyamide-forming monomers in an amount of 15 to 90 weight %.
In another preferred embodiment of the Co-Polymer (C) used according to the invention outlined above the Co-Polymer contains the units derived from polycarbonate diols or polycarbonate diamines in an amount of 15 to 90 weight %.
Another aspect of the invention provides a process for the production of a modified polyamide forming a part of the Co-Polymer used according to the invention, wherein one or more pre-polyamide/s is contacted/mixed with an at least mono-substituted α,ω-di-carboylic acid, preferably at least mono- substituted adipic acid, and then the mixture is heated to a temperature above 150° C.
In another preferred embodiment of the process for the production of a modified polyamide forming a part of the Co-Polymer used according to the invention the at least mono-substituted α,ω-di-carboylic acid, preferably the at least mono- substituted adipic acid is added in an amount resulting in a molar ratio between the acid and the pre-polyamide calculated relatively based on the equivalent number of lactam Units in the pre-polyamide

between 0.05 and 0.0005, preferably between 0.025 and 0.001;
or between 1.0 and 0.0005, preferably between 0.75 and 0.00075, and more preferably between 0.5 and 0.001, or between 0.05 and 0.004, or between 0.1 and 0.001;
or in an amount resulting in a molar ratio between the acid and the pre-polyamide calculated relatively based on molecular weight of the polymerized amide building block (VIII)
- ■ between 0.05 and 0.0005, preferably between 0.025 and 0.001; or
- ■ between 1.0 and 0.0005, preferably between 0.75 and 0.00075, and more preferably between 0.5 and 0.001, or between 0.05 and 0.004, or between 0.1 and 0.001.

In another preferred embodiment of the process for the production of a modified polyamide forming a part of the Co-Polymer used according to the invention the reaction is executed using reactive extrusion.
Another aspect of the current invention provides the use of a Co-Polymer used according to the invention in the production of implants or medical devices, preferably implanted or implantable medical devices, more preferably for the production of balloon/balloon material, of stents, stent grafts, grafts graft connectors or catheters.
As described above a main aspect of the current invention provides implants or medical devices, comprising a Co-Polymer according to the invention, preferably implanted or implantable medical devices, more preferably balloon/balloon material, stents, stent grafts, grafts graft connectors or catheters.
The examples and figures in the following section describing the use of the polyamides are merely illustrative and the invention cannot be considered in any way as being restricted to these applications.

Examples:

A) The following examples A1 to A5 are examples of the production of the modified polyamide forming part of the Co-Polymer according to the invention:

Example A1: (1.4%; normal reaction)

50 g dried Nylon 12 (with a molecular weight of approx. 26000 g/mol) was mixed with 0.688 g (0.0034 mol) 3-tert. butyl adipic acid under argon for 2h at 220° C. The temperature was raised within 20 min to 250 ° C and the mixture was stirred for another 2h. The resulting solid gave a molecular weight of 13000 g/mol. The relative molar ratio (see above) was 0.013, being calculated as 0.0034 mol (acid) : 0.253 rel. mol (Polyamid: MW (building block) 197.3).

Example A2: (1.4%; extrusion)

The reaction of example A1 is carried out in an extruder by way of the so-called (reactive extrusion) as described in DD 276 290 A1 and Eichhorn et al. (Journal of Applied Polymer Science, Vol. 62, 2053-2060 (1996). Reaction time in each of the 2 steps is reduced to below 30 min.

Example A3: (0.5%; normal reaction)

1651 g dried Nylon 12 (with a molecular weight of approx. 26000 g/mol) is mixed with 8.25 g (0.040 mol) 3-tert. butyl adipic acid under argon for 2h at 220° C. The temperature is raised within 20 min to 250° C and the mixture is stirred for another 2h. The relative molar ratio (see above) is 0.0048, being calculated as 0.040 mol (acid) : 8.368 rel. mol (Polyamid: MW (building block) 197.3).

Example A4: (0.25%; normal reaction)

1753 g dried Nylon 12 (with a molecular weight of approx. 26000 g/mol) is mixed with 4.38 g (0.022 mol) 3-tert. butyl adipic acid under argon for 2h at 220° C. The temperature is raised within 20 min to 250° C and the mixture is stirred for another 2h. The relative molar ratio (see above) is 0.0025, being calculated as 0.022 mol (acid) : 8.885 rel. mol (Polyamid: MW (building block) 197.3).

Example A5: (2.0%; normal reaction)

1694 g dried Nylon 12 (with a molecular weight of approx. 26000 g/mol) is mixed with 33.88 g (0.167 mol) 3-tert. butyl adipic acid under argon for 2h at 220° C. The temperature is raised within 20 min to 250 ° C and the mixture is stirred for another 2h. The relative molar ratio (see above) is 0.0195, being calculated as 0.167 mol (acid) : 8.586 rel. mol (Polyamid: MW (building block) 197.3).

C) The following examples C1 or C2 are examples of the production of a Co-Polymer according to the invention:

Example C1: Co-Polymer with Polycarbonate diol

The modified polyamide according to example A1 is mixed with polyhexamethylene-carbonate diol at 200°C and the mixture is stirred for 4h.

Example C2: Co-Polymer with Polycarbonate diamine

The modified polyamide according to example A1 is mixed with polyhexamethylene-carbonate diamine at 200°C and the mixture is stirred for 4h.
In some examples the modified polyamide is mixed with polyhexamethylene-carbonate diol or diamine in a roughly or exactly equimolar amount.
The carbonate diols are commercially available and are well known in the art and thus can also easily be synthesized by someone skilled in the art. Specific carbonate diamines, which may not be commercially available, can be synthesized by someone skilled in the art following and/or adapting the synthetic pathways known in the art. An example is adaptation of the following literature article for producing amino-modified polyethylene-oxides included here by reference: McManus, N. T. et al., Journal of Applied Polymer Science (2006), 101(6), 4230-4237.

Test of mechanical properties:

The material according to examples C1 and C2 are compared to PEBAX®

D) Formation of a Medical Balloon

Example D1: From the Material according to examples C1 and C2 lengths of a polymer tubing are formed by extrusion. The proximal and distal portions of the lengths of tubing are stretched to a reduced diameter while retaining an unstretched central portion, The lengths of polymer tubing are then radially expanded under pressure by expanding the tubing in a mold so that the balloon body is formed from the unstretched central portion of the tubing. The proximal and distal waist portions of the balloon are formed from the stretched proximal and distal portions of the tubing.
Example D2: From the Material according to examples C1 and C2 tubular segments with a predetermined wall thickness and length are formed by extrusion with a proximal end, a distal end and a center portion. The segment is then drawn to a predetermined length while maintaining the temperature of the segment below the highest glass transition temperature of the Co-Polymer according to examples C1 or C2. Thereby the proximal end forms a first waist. Following that, this segment with the first waist is expanded in a mold to produce the balloon. After finishing, the balloon has a body portion, wherein the center portion of the segment forms the balloon body portion.

Claims

Use of a Co-Polymer producible by polymerizing a modified polyamide with a polycarbonate diol or a polycarbonate diamine, characterized in that the modified polyamide is producible by contacting/mixing one or more pre-polyamides with an at least mono-substituted α,ω-di-carboxylic acid or its alkyl ester or its acyl halides and raising the temperature to above 150° C in the production of implants or medical devices.
Use according to claim 1, wherein the at least mono-substituted α,ω-di-carboxylic acid is 3-tert. butyl adipic acid.
Use according to claim 1 wherein the pre-polyamide is a structure of general formula III or IIIa
or
, wherein
A is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;

A' is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;

B and B' independently from one another are selected from H or C_1-4-Alkyl;

v is a natural number between 1 and 24;

v' is a natural number between 1 and 24;

y is a natural number ≥1.
Use according to claim 3 wherein the pre-polyamide is a structure of general formula III.
Use according to claim 1 wherein the pre-polyamide is selected from Nylon 6; Nylon 6,6; Nylon 11; or Nylon 12; preferably is Nylon 12;
and
the at least mono-substituted α,ω-di-carboxylic acid is 3-tert. butyl adipic acid.
Use according to claim 5 wherein the pre-polyamide is Nylon 12;
and
the at least mono-substituted α,ω-di-carboxylic acid is 3-tert. butyl adipic acid.
Use according to claim 1, characterized in that the modified polyamide is of general formula IV or IVa
or
wherein
A is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;

A' is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;

B and B' independently from one another are selected from H or C_1-4-Alkyl;

v is a natural number between 1 and 24;

v' is a natural number between 1 and 24;

y is a natural number ≥1;

y' is a natural number ≥1 or 0;

m and n are independently from each other selected from 0 and a natural number between 1 and 9 and n + m is a natural number between 1 and 9; and

R¹ is any radical except hydrogen, preferably is a sterically voluminous group.
Use according to claim 7, characterized in that the modified polyamide is of general formula IV.
Use according to claim 1, wherein the polycarbonate is a polycarbonate diol of general formula VI or VIa

or the polycarbonate is a polycarbonate diamine of general formula VII or VIIa

, wherein
E is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain;

B and B' independently from one another are selected from H or C_1-4-Alkyl;

w is a natural number between 1 and 24;

z is a natural number ≥1.
Use according to any of claims 1 to 9, wherein
• either the reaction leading to the modified polyamide; or

• the polymerization reaction; or

• both reactions
is/are executed using reactive extrusion.
Use of a Co-Polymer according to general formula X, Xa, Xb or Xc, or XI, XIa, XIb or XIc
or
or
or

or
or
or
, wherein
A is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;

A' is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;

E is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain;

B and B' independently from one another are selected from H or C_1-4-Alkyl;

v is a natural number between 1 and 24;

v' is a natural number between 1 and 24;

w is a natural number between 1 and 24;

x is a natural number ≥1;

y and y' are independently from one another a natural number ≥1;

z is a natural number ≥1;

m and n are independently from each other selected from 0 and a natural number between 1 and 9 and n + m is a natural number between 1 and 9; and

R¹ is any radical except hydrogen, preferably is a sterically voluminous group

in the production of implants or medical devices..
Use according to claim 11, wherein
v is 11;

and

R¹ is tert. butyl.
Use of a Co-Polymer comprising units derived from polyamide-forming monomers, units derived from polycarbonate diols or polycarbonate diamines and units derived from at least mono-substituted α,ω-di-carboxylic acids,
wherein the polyamide-forming monomers are represented by the following formulas (IX) or (IXa), the polycarbonate diols are represented by the following formulas (VI) or (VIa), polycarbonate diamines are represented by the following formula (VII) or (VIIa) and the at least mono-substituted α,ω-di-carboxylic acids are represented by the following formula (I):
, wherein
A is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain, with optionally one carbon atom being replaced by NH, O or S;
and

v is a natural number between 1 and 24;
with

or

, wherein

E is a divalent, branched or linear, saturated or non-saturated, optionally substituted hydrocarbon chain;

B and B' independently from one another are selected from H or C_1-4-Alkyl;

w is a natural number between 1 and 24;

z is a natural number ≥1;
with

HOOC-(CH₂)_m-CHR¹-(CH₂)_n-COR² (I)

wherein

m and n are independently from each other selected from a natural number and 0 and n + m is between 1 and 9, or between 3 and 7;

R² is selected from OH, halogen or OC_1-4-alkyl;

R¹ is any radical except hydrogen, preferably is a sterically voluminous group

in the production of implants or medical devices.
Use of a Co-Polymer according to any of claims 1 to 13 wherein the implants or medical devices are implanted or implantable medical devices
Use of a Co-Polymer according to any of claims 1 to 14 wherein the implants or medical devices are balloon/balloon material, of stents, stent grafts, grafts graft connectors or catheters.